Journal
CLINICAL SCIENCE
Volume 116, Issue 11-12, Pages 837-850Publisher
PORTLAND PRESS LTD
DOI: 10.1042/CS20080484
Keywords
alpha(1)-antitrypsin; chronic obstructive pulmonary disease (COPD); endoplasmic reticulum; proteolytic cascade; serine protease inhibitor; serpinopathy
Categories
Funding
- Medical Research Council [60500306, 6070099]
- Medical Research Council (MRC) Clinical Research Fellowship [60601403, 60601840, 60501381]
- Wellcome Trust Intermediate Clinical Fellowship
- Wennergren Foundation (Sweden)
- Swedish Society for Medical Research (SSMF)
- MRC [G0601840, G0601403, G0700990, G0500306] Funding Source: UKRI
- Medical Research Council [G0601403, G0601840, G0500306, G0700990] Funding Source: researchfish
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alpha(1)-Antitrypsin is the prototypical member of the serine proteinase inhibitor or serpin superfamily of proteins. The family includes alpha(1)-antichymotrypsin, CI inhibitor, antithrombin and neuroserpin, which are all linked by a common molecular structure and the same suicidal mechanism for inhibiting their target enzymes. Point mutations result in an aberrant conformational transition and the formation of polymers that are retained within the cell of synthesis. The intracellular accumulation of polymers of mutant alpha(1)-antitrypsin and neuroserpin results in a toxic gain-of-function phenotype associated with cirrhosis and dementia respectively. The lack of important inhibitors results in overactivity of proteolytic cascades and diseases such as COPD (chronic obstructive pulmonary disease) (alpha(1)-antitrypsin and alpha(1)-antichymotrypsin), thrombosis (antithrombin) and angio-oedema (CI inhibitor). We have grouped these conditions that share the same underlying disease mechanism together as the serpinopathies. In the present review, the molecular and pathophysiological basis of alpha(1)-antitrypsin deficiency and other serpinopathies are considered, and we show how understanding this unusual mechanism of disease has resulted in the development of novel therapeutic strategies.
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